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Derivatives 2 - pyrrolidin-3-yl - 1H imidazole, as nonstructural 5a Protein inhibitors of hepatitis C virus

机译:衍生物2-吡咯烷-3-基-1H咪唑,作为丙型肝炎病毒的非结构性5a蛋白抑制剂

摘要

Refers to a compound of formula (i) where a is a single link, imidazole, thiazole, benzimidazole, among others; b and B 'are together pirrolo [1,2-b] pyridazine hydrochloride, indolizina, pirrolo [1,2-c] pyrimidine; imidazo [1,2-a] pyrimidine, among others; W pyrrole is Preferred; and', and are each C, N; Z and Z ' Each one is H, alkyl C8 heteroalquilo C1 C1, C8, cycloalkyl, aryl, among others; ra's Oh, CN,NO2, halogen, alkyl of C1 - C12, among others, RC, RD, re and RF are each h, alkyl C8 heteroalquilo C1 C1, C8, aralquilo, cycloalkyl, among others; R is independently an integer of 0 - 3. Also referred to a Pharmaceutical composition. Said Compound is nonstructural 5a Protein inhibitor used in the treatment of hepatitis C
机译:指其中a为单键的式(i)化合物,咪唑,噻唑,苯并咪唑等; b和B′一起是吡咯罗[1,2-b]哒嗪盐酸盐,吲哚嗪,吡咯罗[1,2-c]嘧啶;咪唑并[1,2-a]嘧啶等;优选W吡咯;和',并且分别为C,N; Z和Z′各自为H,烷基,C8,杂芳基,C1,C1,C8,环烷基,芳基等。 ra的哦,CN,NO 2,卤素,C 1 -C 12的烷基,其中RC,RD,re和RF分别为h,烷基C 8杂芳基C 1,C 8,芳基,环烷基等。 R独立地是0-3的整数。也称为药物组合物。所述化合物是用于治疗丙型肝炎的非结构性5a蛋白抑制剂

著录项

  • 公开/公告号PE01242012A1

    专利类型

  • 公开/公告日2012-03-17

    原文格式PDF

  • 申请/专利权人 PRESIDIO PHARMACEUTICALS INC.;

    申请/专利号PE20110001154

  • 发明设计人 LI LEPING;ZHONG MIN;

    申请日2009-12-02

  • 分类号A01N57/00;A61K31/675;

  • 国家 PE

  • 入库时间 2022-08-21 17:23:25

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